PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
25549925-5	2015	Among them, luteolin (2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one) showed the most potent inhibition (IC5095nM), which is also more potent compared to all known classes of CBR1 inhibitors.	Luteolin	12-20	carbonyl reductase 1	Homo sapiens	188-192	
25549925-5	2015	Among them, luteolin (2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one) showed the most potent inhibition (IC5095nM), which is also more potent compared to all known classes of CBR1 inhibitors.	Luteolin	22-81	carbonyl reductase 1	Homo sapiens	188-192	
26415702-8	2015	Some polyphenols (e.g. luteolin, apigenin and curcumin) have been shown to be very potent CBR1 inhibitors.	Luteolin	23-31	carbonyl reductase 1	Homo sapiens	90-94